Azeotrope-like compositions of 1,1,2,3,3-pentafluoropropene

ABSTRACT

The invention pertains to azeotrope-like compositions of 1,1,2,3,3-pentafluoropropene (HFC-1225yc) and any one of 1,1,1,2-tetrafluoropropene (HFC-1234yf) or the Z-isomer of 1,1,1,2,3-pentafluoropropene (HFC-1225yeZ), and uses thereof, including use in refrigerant compositions, refrigeration systems, blowing agent compositions, and aerosol propellants.

BACKGROUND OF THE INVENTION

1. Field of Invention

The invention pertains to azeotrope-like compositions of 1,1,2,3,3-pentafluoropropene (HFO-1225yc) and any one of 1,1,1,2-tetrafluoropropene (HFO-1234yf) or the Z-isomer of 1,1,1,2,3-pentafluoropropene (HFO-1225yeZ), and uses thereof.

2. Description of the Related Art

Fluorocarbon based fluids have found widespread use in industry in a number of applications, including as refrigerants, aerosol propellants, blowing agents, heat transfer media, and gaseous dielectrics. Because of the suspected environmental problems associated with the use of some of these fluids, including the relatively high global warming potentials associated therewith, it is desirable to use fluids having low or even zero ozone depletion potential. Thus, the use of fluids that do not contain chlorofluorocarbons (“CFCs”) or hydrochlorofluorocarbons (“HCFCs”) is desirable. Compounds having a low ozone depletion potential include hydrofluorocarbons (“HFCs”), especially hydrofluoroolefins (“HFO's”). Compounds having a low global warming potential are also desirable. In this regard, the use of alkenes is also desirable due to their short atmospheric lifetime which results in a relatively low global warming potential. Additionally, the use of single component fluids or azeotropic mixtures, which do not fractionate on boiling and evaporation, is desirable. However, the identification of new, environmentally safe, non-fractionating mixtures is complicated due to the fact that azeotrope formation is not readily predictable.

The industry is continually seeking new fluorocarbon based mixtures that offer alternatives, and are considered environmentally safer substitutes for CFCs and HCFCs. Of particular interest are mixtures containing hydrofluorocarbons, fluoroolefins and other fluorinated compounds, which have a low ozone depletion potentials and low global warming potential. Such mixtures are the subject of this invention.

U.S. Pat. No. 6,858,571 describes azeotrope-like compositions comprising pentafluoropropene (HFO-1225) and a fluid selected from the group consisting of 3,3,3-trifluoropropene (“HFO-1243zf”), 11-difluoroethane (“HFC-152a”), trans-1,3,3,3-tetrafluoropropene (“HFO-1234ze”), and combinations of two or more thereof. However, U.S. Pat. No. 6,858,571 does not show azeotrope-like composition comprising HFO-1225yc with either HFO-1234yf or HFO-1225yeZ. The invention concerns compositions that help to satisfy the continuing need for alternatives to CFCs and HCFCs. The compositions of the invention exhibit relatively low global warming potentials (“GWP”). Accordingly, applicants have recognized that such compositions can be used to great advantage in a number of applications, including as replacements for CFCs, HCFC's, and HFCs in refrigerant, aerosol, blowing agents, and other applications.

DETAILED DESCRIPTION OF THE INVENTION

Accordingly, the present invention provides azeotrope-like compositions comprising 1,1,2,3,3-pentafluoropropene (HFO-1225yc) and any one of 1,1,1,2-tetrafluoropropene (HFO-1234yf) or the Z-isomer of 1,1,1,2,3-pentafluoropropene (HFO-1225yeZ). One embodiment of the invention provides an azeotrope-like composition comprising 1,1,2,3,3-pentafluoropropene and, 1,1,1,2-tetrafluoropropene. Another embodiment of the invention provides an azeotrope-like composition comprising 1,1,2,3,3-pentafluoropropene and the Z-isomer of 1,1,1,2,3-pentafluoropropene. The azeotrope-like compositions of the present invention exhibits properties that make that make them advantageous for use as, or in, a refrigerant, an aerosol, and blowing agent compositions.

The invention further provides a method for modifying a refrigeration apparatus which refrigeration apparatus comprises a refrigerant, which refrigerant comprises a combination of a chlorofluorocarbon or a hydrochlorofluorocarbon and a mineral oil, comprising removing at least a portion of the chlorofluorocarbon or hydrochlorofluorocarbon from the refrigerant and leaving a residue comprising the mineral oil, and adding to said residue an azeotrope-like composition comprising 1,1,2,3,3-pentafluoropropene and any one of 1,1,1,2-tetrafluoropropene or the Z-isomer of 1,1,1,2,3-pentafluoropropene.

As used herein, the term “azeotrope-like” is intended in its broad sense to include both compositions that are strictly azeotropic and compositions that behave like azeotropic mixtures. From fundamental principles, the thermodynamic state of a fluid is defined by pressure, temperature, liquid composition, and vapor composition. An azeotropic mixture is a system of two or more components in which the liquid composition and vapor composition are equal at the stated pressure and temperature. In practice, this means that the components of an azeotropic mixture are constant boiling and cannot be separated during a phase change. The azeotrope-like compositions of the invention may include additional components that do not form new azeotrope-like systems, or additional components that are not in the first distillation cut. The first distillation cut is the first cut taken after the distillation column displays steady state operation under total reflux conditions. One way to determine whether the addition of a component forms a new azeotrope-like system so as to be outside of this invention is to distill a sample of the composition with the component under conditions that would be expected to separate a non-azeotropic mixture into its separate components. If the mixture containing the additional component is non-azeotrope-like, the additional component will fractionate from the azeotrope-like components. If the mixture is azeotrope-like, some finite amount of a first distillation cut will be obtained that contains all of the mixture components that is constant boiling or behaves as a single substance. It follows from this that another characteristic of azeotrope-like compositions is that there is a range of compositions containing the same components in varying proportions that are azeotrope-like or constant boiling. All such compositions are intended to be covered by the terms “azeotrope-like” and “constant boiling”. As an example, it is well known that at differing pressures, the composition of a given azeotrope will vary at least slightly, as does the boiling point of the composition. Thus, an azeotrope of A and B represents a unique type of relationship, but with a variable composition depending on temperature and/or pressure. It follows that, for azeotrope-like compositions, there is a range of compositions containing the same components in varying proportions that are azeotrope-like. All such compositions are intended to be covered by the term azeotrope-like as used herein. It is well recognized in the art that it is not possible to predict the formation of azeotropes. (See, for example, U.S. Pat. No. 5,648,017 (column 3, lines 64-65) and U.S. Pat. No. 5,182,040 (column 3, lines 62-63), both of which are incorporated herein by reference). It has been unexpectedly discovered that 1,1,2,3,3-pentafluoropropene (HFO-1225yc) and any one of 1,1,1,2-tetrafluoropropene (HFO-1234yf) or the Z-isomer of 1,1,1,2,3-pentafluoropropene (HFO-1225yeZ), form azeotrope-like compositions.

According to certain preferred embodiments, the azeotrope-like compositions of the present invention comprise, and preferably consist essentially of, effective amounts of 1,1,2,3,3-pentafluoropropene (HFO-1225yc) and any one of 1,1,1,2-tetrafluoropropene (HFO-1234yf) or the Z-isomer of 1,1,1,2,3-pentafluoropropene (HFO-1225yeZ). The term “effective amounts” as used herein refers to the amount of each component which upon combination with the other component, results in the formation of an azeotrope-like composition of the present invention.

The azeotrope-like compositions of the present invention can be produced by combining effective amounts of 1,1,2,3,3-pentafluoropropene (HFO-1225yc) and any one of 1,1,1,2-tetrafluoropropene (HFO-1234yf) or the Z-isomer of 1,1,1,2,3-pentafluoropropene (HFO-1225yeZ). Any of a wide variety of methods known in the art for combining two or more components to form a composition can be adapted for use in the present methods to produce an azeotrope-like composition. For example, the 1,1,2,3,3-pentafluoropropene (HFO-1225yc) and any one of 1,1,1,2-tetrafluoropropene (HFO-1234yf) or the Z-isomer of 1,1,1,2,3-pentafluoropropene (HFO-1225yeZ), can be mixed, blended, or otherwise contacted by hand and/or by machine, as part of a batch or continuous reaction and/or process, or via combinations of two or more such steps. In light of the disclosure herein, those skilled in the art will be readily able to prepare azeotrope-like compositions according to the present invention without undue experimentation.

The 1,1,2,3,3-pentafluoropropene (HFO-1225yc) and any one of 1,1,1,2-tetrafluoropropene (HFO-1234yf) or the Z-isomer of 1,1,1,2,3-pentafluoropropene (HFO-1225yeZ) are present in amounts effective to produce an azeotrope-like composition. In one embodiment the 1,1,2,3,3-pentafluoropropene (HFO-1225yc) is present in the azeotrope-like composition in an amount of from greater than zero to about 25 weight percent, preferably from greater than zero to about 20 weight percent, and more preferably from about 2 to about 15 weight percent. In one embodiment the 1,1,1,2-tetrafluoropropene (HFO-1234yf) or the Z-isomer of 1,1,1,2,3-pentafluoropropene (HFO-1225yeZ) is present in the azeotrope-like composition in an amount of from about 75 to less than 100 weight percent, preferably from about 80 to less than 100 weight percent, and more preferably from about 85 to about 98 weight percent.

The azeotrope-like composition of 1,1,2,3,3-pentafluoropropene and 1,1,1,2-tetrafluoropropene has a boiling point at about 14.5 psia of from about −29° C. to about −27.5° C.; preferably from about −29° C. to about −28° C.

The azeotrope-like composition of 1,1,2,3,3-pentafluoropropene and the Z-isomer of 1,1,1,2,3-pentafluoropropene has a boiling point at about 14.5 psia of from about −19.2° C. to about −188.9, preferably from about −19.2° C. to about −19° C.

The present azeotrope-like compositions have utility in a wide range of applications. For example, as a blowing agent, as part of a sprayable composition such as an aerosol composition, as cleaning composition, or a refrigerant composition.

Yet another embodiment of the present invention relates to a blowing agent comprising one or more azeotrope-like compositions of the invention. One embodiment of the present invention relates to methods of forming thermoset foams, and preferably polyurethane and polyisocyanurate foams. The methods generally comprise providing a blowing agent composition of the present inventions, directly or indirectly adding the blowing agent composition to a foamable composition, and reacting the foamable composition under the conditions effective to form a foam or cellular structure, as is well known in the art. These comprise a foamable composition comprising the azeotrope-like composition above and at least one thermoset foam component. For example, the thermoset foam component may comprise a composition capable of forming a polyurethane foam, a polyisocyanurate foam or a phenolic foam. It is possible to produce thermoplastic foams using the compositions of the invention. These foams may be open cell or closed cell. Any of the methods well known in the art, such as those described in “Polyurethanes Chemistry and Technology,” Volumes I and II, Saunders and Frisch, 1962, John Wiley and Sons, New York, N.Y., which is incorporated herein by reference, may be used or adapted for use in accordance with the foam embodiments of the present invention.

In general, polyurethane or polyisocyanurate foams are prepared by combining an isocyanate, the polyol premix composition, and other materials such as optional flame retardants, colorants, or other additives. These foams can be rigid, flexible, or semi-rigid, and can have a closed cell structure, an open cell structure or a mixture of open and closed cells. In general, such preferred methods comprise preparing polyurethane or polyisocyanurate foams by combining an isocyanate, a polyol or mixture of polyols, a blowing agent or mixture of blowing agents comprising one or more of the present compositions, and other materials such as catalysts, surfactants, and optionally, flame retardants, colorants, or other additives.

It is convenient in many applications to provide the components for polyurethane or polyisocyanurate foams in pre-blended formulations. Most typically, the foam formulation is pre-blended into two components. The isocyanate and optionally certain surfactants and blowing agents comprise the first component, commonly referred to as the “A” component. The polyol or polyol mixture, a surfactant including silicone surfactants, catalysts including amine catalysts, blowing agents, flame retardant, and other isocyanate reactive components comprise the second component, commonly referred to as the “B” component. The blowing agent comprises the azeotrope-like composition of this invention and optionally a hydrocarbon, halogenated hydrocarbon, CO₂ generating material, or combinations thereof. Preferably the halogenated hydrocarbon comprises a chlorofluorocarbon, hydrochlorofluorocarbon, hydrofluorocarbon, or combinations thereof. The blowing agent component is usually present in the polyol premix composition in an amount of from about 1 wt. % to about 30 wt. %, by weight of the polyol premix composition. The polyol component, can be any polyol which reacts in a known fashion with an isocyanate in preparing a polyurethane or polyisocyanurate foam. Useful polyols comprise one or more of a sucrose containing polyol; phenol, a phenol formaldehyde containing polyol; a glucose containing polyol; a sorbitol containing polyol; a methylglucoside containing polyol; an aromatic polyester polyol; glycerol; ethylene glycol; diethylene glycol; propylene glycol; graft copolymers of polyether polyols with a vinyl polymer; a copolymer of a polyether polyol with a polyurea; or combinations thereof. The polyol component is usually present in the polyol premix composition in an amount of from about 60 wt. % to about 95 wt. %, by weight of the polyol premix composition. The polyol premix composition next contains a surfactant component which silicone surfactant and optionally an additional non-silicone surfactant. The surfactant is usually present in the polyol premix composition in an mount of from about 0.5 wt. % to about 5.0 wt. % by weight of the polyol premix composition. The polyol premix composition next contains a catalyst which is preferably an amine. Tertiary amines are preferred. Preferred amines include: N,N-dimethylcyclohexylamine, dimethlyethanolamine, N,N,N′,N′,N″,N″-pentamethyldiethylenetriamine, 1,4-diaza-bicyclo[2.2.2]octane (DABCO), and triethylamine. The catalyst is usually present in the polyol premix composition in an amount of from about 0.1 wt. % to about 3.5 wt. % by weight of the polyol premix composition.

A foamable composition suitable for forming a polyurethane or polyisocyanurate foam may be formed by reacting an organic polyisocyanate and the polyol premix composition described above. Any organic polyisocyanate can be employed in polyurethane or polyisocyanurate foam synthesis inclusive of aliphatic and aromatic polyisocyanates. Suitable organic polyisocyanates include aliphatic, cycloaliphatic, araliphatic, aromatic, and heterocyclic isocyanates which are well known in the field of polyurethane chemistry. These are described in, for example, U.S. Pat. Nos. 4,868,224; 3,401,190; 3,454,606; 3,277,138; 3,492,330; 3,001,973; 3,394,164; 3,124.605; and 3,201,372. Preferred as a class are the aromatic polyisocyanates. Representative organic polyisocyanates correspond to the formula: R(NCO)z wherein R is a polyvalent organic radical which is either aliphatic, aralkyl, aromatic or mixtures thereof, and z is an integer which corresponds to the valence of R and is at least two.

Accordingly, polyurethane or polyisocyanurate foams are readily prepared by bringing together the A and B side components either by hand mix for small preparations and, preferably, machine mix techniques to form blocks, slabs, laminates, pour-in-place panels and other items, spray applied foams, froths, and the like. Optionally, other ingredients such as fire retardants, colorants, auxiliary blowing agents, and even other polyols can be added as a third stream to the mix head or reaction site. Most preferably, however, they are all incorporated into one B-component as described above. Conventional flame retardants can also be incorporated, preferably in amount of not more than about 20 percent by weight of the reactants.

In addition to the previously described ingredients, other ingredients such as, dyes, fillers, pigments and the like can be included in the preparation of the foams. Dispersing agents and cell stabilizers can be incorporated into the present blends. Conventional fillers for use herein include, for example, aluminum silicate, calcium silicate, magnesium silicate, calcium carbonate, barium sulfate, calcium sulfate, glass fibers, carbon black and silica. The filler, if used, is normally present in an amount by weight ranging from about 5 parts to 100 parts per 100 parts of polyol. A pigment which can be used herein can be any conventional pigment such as titanium dioxide, zinc oxide, iron oxide, antimony oxide, chrome green, chrome yellow, iron blue siennas, molybdate oranges and organic pigments such as para reds, benzidine yellow, toluidine red, toners and phthalocyanines. The polyurethane or polyisocyanurate foams produced can vary in density from about 0.5 pounds per cubic foot to about 60 pounds per cubic foot, preferably from about 1.0 to 20.0 pounds per cubic foot, and most preferably from about 1.5 to 6.0 pounds per cubic foot. The density obtained is a function of how much of the blowing agent or blowing agent mixture disclosed in this invention plus the amount of auxiliary blowing agent, such as water or other co-blowing agents is present in the A and/or B components, or alternatively added at the time the foam is prepared. These foams can be rigid, flexible, or semi-rigid foams, and can have a closed cell structure, an open cell structure or a mixture of open and closed cells. These foams are used in a variety of well known applications, including but not limited to thermal insulation, cushioning, flotation, packaging, adhesives, void filling, crafts and decorative, and shock absorption.

The invention also contemplates forming a thermoplastic form. For example, conventional polystyrene and polyethylene formulations may be combined with the azeotrope-like composition in a conventional manner to produce thermoplastic foams. Examples of thermoplastic foam components include polyolefins, such as for example polystyrene. Other examples of thermoplastic resins include polyethylene, ethylene copolymers, polypropylene, and polyethyleneterephthalate. In certain embodiments, the thermoplastic foamable composition is an extrudable composition. It is also generally recognized that the thermoplastic foamable composition may include adjuvants such as nucleating agents, flame or fire retardant materials, cell modifiers, cell pressure modifiers, and the like.

With respect to thermoplastic foams, the preferred methods generally comprise introducing a blowing agent in accordance with the present invention into a thermoplastic material, and then subjecting the thermoplastic material to conditions effective to cause foaming. For example, the step of introducing the blowing agent into the thermoplastic material may comprise introducing the blowing agent into a screw extruder containing a thermoplastic polymer, and the step of causing foam may comprise lowering the pressure on the thermoplastic material and thereby causing expansion of the blowing agent and contributing to the foaming of the material. Suitable thermoplastic polymers non-exclusively include polystyrene, polyethylene, polypropylene, polyethylene terephthalate, and combinations of these. It will be generally appreciated by those skilled in the art, especially in view of the disclosure herein, that the order and manner in which the blowing agent of the present invention is formed and/or added to the foamable composition does not generally affect the operability of the present invention thermoset or thermoplastic foams. It is contemplated also that in certain embodiments it may be desirable to utilize the present compositions when in the supercritical or near supercritical state as a blowing agent.

The azeotrope-like compositions of this invention may also be used as refrigerant compositions. The refrigerant compositions of the present invention may be used in any of a wide variety of refrigeration systems including air-conditioning, refrigeration, heat-pump systems, and the like. In certain preferred embodiments, the compositions of the present invention are used in refrigeration systems originally designed for use with an HFC-refrigerant, such as, for example, HFC-134a. The preferred compositions of the present invention tend to exhibit many of the desirable characteristics of HFC-134a and other HFC-refrigerants, including non-flammability, and a GWP that is as low, or lower than that of conventional HFC-refrigerants. In addition, the relatively constant boiling nature of the compositions of the present invention makes them even more desirable than certain conventional HFCs for use as refrigerants in many applications.

In certain other preferred embodiments, the present compositions are used in refrigeration systems originally designed for use with a CFC-refrigerant. Preferred refrigeration compositions of the present invention may be used in refrigeration systems containing a lubricant used conventionally with CFC-refrigerants, such as mineral oils, silicone oils, and the like, or may be used with other lubricants traditionally used with HFC refrigerants. In certain embodiments, the compositions of the present invention may be used to retrofit refrigeration systems containing HFC, HCFC, and/or CFC-refrigerants and lubricants used conventionally therewith. Preferably, the present methods involve recharging a refrigerant system that contains a refrigerant to be replaced and a lubricant comprising the steps of (a) removing at least a portion of the refrigerant to be replaced from the refrigeration system while retaining a substantial portion of the lubricant in said system; and (b) introducing to the system a composition of the present invention. As used herein, the term “substantial portion” refers generally to a quantity of lubricant which is at least about 50% by weight of the quantity of lubricant contained in the refrigeration system prior to removal of the chlorine-containing refrigerant. Preferably, the substantial portion of lubricant in the system according to the present invention is a quantity of at least about 60% of the lubricant contained originally in the refrigeration system, and more preferably a quantity of at least about 70%. As used herein the term “refrigeration system” refers generally to any system or apparatus, or any part or portion of such a system or apparatus, which employs a refrigerant to provide cooling. Such refrigeration systems include, for example, air conditioners, electric refrigerators, chillers, transport refrigeration systems, commercial refrigeration systems and the like.

Any of a wide range of known methods can be used to remove refrigerants to be replaced from a refrigeration system while removing less than a major portion of the lubricant contained in the system. For example, because refrigerants are quite volatile relative to traditional hydrocarbon-based lubricants where the boiling points of refrigerants are generally less than 10° C. whereas the boiling points of mineral oils are generally more than 200° C. In embodiments wherein the lubricant is a hydrocarbon-based lubricant, the removal step may readily be performed by pumping chlorine-containing refrigerants in the gaseous state out of a refrigeration system containing liquid state lubricants. Such removal can be achieved in any of a number of ways known in the art, including, the use of a refrigerant recovery system, such as the recovery system manufactured by Robinair of Ohio. Alternatively, a cooled, evacuated refrigerant container can be attached to the low pressure side of a refrigeration system such that the gaseous refrigerant is drawn into the evacuated container and removed. Moreover, a compressor may be attached to a refrigeration system to pump the refrigerant from the system to an evacuated container. In light of the above disclosure, those of ordinary skill in the art will be readily able to remove chlorine-containing lubricants from refrigeration systems and to provide a refrigeration system having therein a hydrocarbon-based lubricant and substantially no chlorine-containing refrigerant according to the present invention.

Any of a wide range of methods for introducing the present refrigerant compositions to a refrigeration system can be used in the present invention. For example, one method comprises attaching a refrigerant container to the low-pressure side of a refrigeration system and turning on the refrigeration system compressor to pull the refrigerant into the system. In such embodiments, the refrigerant container may be placed on a scale such that the amount of refrigerant composition entering the system can be monitored. When a desired amount of refrigerant composition has been introduced into the system, charging is stopped. Alternatively, a wide range of charging tools, known to those of skill in the art, is commercially available. Accordingly, in light of the above disclosure, those of skill in the art will be readily able to introduce the refrigerant compositions of the present invention into refrigeration systems according to the present invention without undue experimentation.

According to certain other embodiments, the present invention provides refrigeration systems comprising a refrigerant of the present invention and methods of producing heating or cooling by condensing and/or evaporating a composition of the present invention. In certain preferred embodiments, the methods for cooling an article according to the present invention comprise condensing a refrigerant composition comprising an azeotrope-like composition of the present invention and thereafter evaporating said refrigerant composition in the vicinity of the article to be cooled. Certain preferred methods for heating an article comprise condensing a refrigerant composition comprising an azeotrope-like composition of the present invention in the vicinity of the article to be heated and thereafter evaporating said refrigerant composition. In light of the disclosure herein, those of skill in the art will be readily able to heat and cool articles according to the present inventions without undue experimentation.

In another embodiment, the azeotrope-like compositions of this invention may be used as propellants in sprayable compositions, either alone or in combination with known propellants. The propellant composition comprises, more preferably consists essentially of, and, even more preferably, consists of the azeotrope-like compositions of the invention. The active ingredient to be sprayed together with inert ingredients, solvents, and other materials may also be present in the sprayable mixture. Preferably, the sprayable composition is an aerosol. Suitable active materials to be sprayed include, without limitation, cosmetic materials such as deodorants, perfumes, hair sprays, cleansers, defluxing agents, and polishing agents as well as medicinal materials such as anti-asthma and anti-halitosis medications. Other uses of the present azeotrope-like compositions include use as solvents, cleaning agents, and the like. Those skilled in the art will be readily able to adapt the present compositions for use in such applications without undue experimentation.

EXAMPLES

The following non-limiting examples serve to illustrate the invention.

Example 1

An ebulliometer consisting of vacuum jacketed tube with a condenser on top which is further equipped with a Quartz Thermometer is used. About 9.54 g HFO-1234yf is charged to the ebulliometer and then HFO-1225yc is added in small, measured increments. Temperature depression is observed when HFO-1225yc is added to HFO-1234yf, indicating a binary minimum boiling azeotrope is formed. From greater than about 0 to about 21 weight percent HFO-1225yc, the boiling point of the composition stays below or around the boiling point of HFO-1234yf. The boiling temperature of HFO-1225yc is about 2° C. at 14.71 psia. The binary mixtures shown in Table 1 were studied and the boiling point of the compositions did not go above the boiling point of HFO-1234 yf. The compositions exhibit azeotrope and/or azeotrope-like properties over this range.

TABLE 1 HFO-1234yf/HFO-1225yc compositions at 14.7 psia Wt. % Wt. % T (° C.) HFO-1234yf HFO-1225yc −27.860 100.00 0.00 −28.435 99.58 0.42 −28.691 98.55 1.45 −28.873 97.15 2.85 −28.871 94.55 5.45 −28.763 92.62 7.38 −28.649 91.38 8.62 −28.482 89.33 10.67 −28.349 87.44 12.56 −28.090 81.75 18.25 −27.742 78.91 21.09 −27.529 76.75 23.25 −27.182 73.44 26.56 −26.966 68.49 31.51 −26.820 61.95 38.05 −26.572 59.74 40.26

Example 2 Comparative

An ebulliometer consisting of vacuum jacketed tube with a condenser on top which is further equipped with a Quartz Thermometer is used. About 17.92 g 1,3,3,3-tetrafluoropropene (trans-HFO-1234ze) is charged to the ebulliometer and then HFO-1225yc is added in small, measured increments. Temperature depression is observed when HFO-1225yc is added to Trans-1234ze, indicating a binary minimum boiling azeotrope is formed. From greater than about 0 to about 7 weight percent HFO-1225yc, the boiling point of the composition stays below or around the boiling point of Trans-1234ze. The binary mixtures shown in Table 2 were studied and the boiling point of the compositions did not go above the boiling point of Trans-1234ze. The compositions exhibit azeotrope and/or azeotrope-like properties over this range.

TABLE 2 Trans-1234ze/1225yc compositions at 14.5 psia Wt. % Wt. % T (° C.) Trans-HFO-1234ze HFO-1225yc −18.353 100.00 0.00 −18.420 99.01 0.99 −18.461 96.66 3.34 −18.458 95.43 4.57 −18.315 92.81 7.19

Example 3

An ebulliometer consisting of vacuum jacketed tube with a condenser on top which is further equipped with a Quartz Thermometer is used. About 19.57 g HFO-1225yeZ is charged to the ebulliometer and then HFO-1225yc is added in small, measured increments. Temperature depression is observed when HFO-1225yc is added to HFO-1225yeZ, indicating a binary minimum boiling azeotrope is formed. From greater than about 0 to about 5 weight percent HFO-1225yc, the boiling point of the composition stays below or around the boiling point of HFO-1225yeZ. The binary mixtures shown in Table 3 were studied and the boiling point of the compositions did not go above the boiling point of HFO-1225yeZ. The compositions exhibit azeotrope and/or azeotrope-like properties over this range.

TABLE 3 HFO-1225yeZ/HFO-1225yc compositions at 14.5 psia Wt. % Wt. % T (° C.) HFO-225yeZ HFO-1225yc −18.854 100.00 0.00 −18.909 98.89 1.11 −18.989 97.56 2.44 −19.154 96.07 3.93 −19.124 95.37 4.63

Example 4 Comparative

An ebulliometer consisting of vacuum jacketed tube with a condenser on top which is further equipped with a Quartz Thermometer is used. About 15.11 g 3,3,3-trifluoropropene is charged to the ebulliometer and then HFO-1225yc is added in small, measured increments. Temperature depression is observed when HFO-1225yc is added to 3,3,3-trifluoropropene, indicating a binary minimum boiling azeotrope is formed. From greater than about 0 to about 10 weight percent HFO-1225yc, the boiling point of the composition stays below or around the boiling point of 3,3,3-trifluoropropene. The binary mixtures shown in Table 4 were studied and the boiling point of the compositions did not go above the boiling point of 3,3,3-trifluoropropene. The compositions exhibit azeotrope and/or azeotrope-like properties over this range.

TABLE 4 3,3,3-trifluoropropene/HFO-1225yc compositions at 14.5 psia Wt. % Wt. % T (° C.) 3,3,3-trifluoropropene HFO-1225yc −24.601 100.00 0.00 −24.607 99.87 0.13 −24.877 95.51 4.49 −24.864 93.50 6.50 −24.646 89.20 10.80

While the present invention has been particularly shown and described with reference to preferred embodiments, it will be readily appreciated by those of ordinary skill in the art that various changes and modifications may be made without departing from the spirit and scope of the invention. It is intended that the claims be interpreted to cover the disclosed embodiment, those alternatives which have been discussed above and all equivalents thereto. 

1. An azeotrope-like composition consisting essentially of 1,1,2,3,3-pentafluoropropene and any one of 1,1,1,2-tetrafluoropropene or the Z-isomer of 1,1,1,2,3-pentafluoropropene.
 2. The azeotrope-like composition of claim 1 consisting essentially of 1,1,2,3,3-pentafluoropropene and 1,1,1,2-tetrafluoropropene.
 3. The azeotrope-like composition of claim 1 consisting essentially of 1,1,2,3,3-pentafluoropropene and the Z-isomer of 1,1,1,2,3-pentafluoropropene.
 4. The azeotrope-like composition of claim 1 which consists essentially of from greater than zero to about 25 weight percent 1,1,2,3,3-pentafluoropropene and from about 75 to less than 100 weight percent of 1,1,1,2-tetrafluoropropene or the Z-isomer of 1,1,1,2,3-pentafluoropropene.
 5. The azeotrope-like composition of claim 1 which consists essentially of from greater than zero to about 20 weight percent 1,1,2,3,3-pentafluoropropene and from about 80 to less than 100 weight percent of 1,1,1,2-tetrafluoropropene or the Z-isomer of 1,1,1,2,3-pentafluoropropene.
 6. The azeotrope-like composition of claim 1 which consists essentially of from about 2 to about 15 weight percent 1,1,2,3,3-pentafluoropropene and from about 85 to about 98 weight percent of 1,1,1,2-tetrafluoropropene or the Z-isomer of 1,1,1,2,3-pentafluoropropene.
 7. The azeotrope-like composition of claim 2 having a boiling point of from about −29° C. to about −27.5° C. at a pressure of about 14.5 psia.
 8. The azeotrope-like composition of claim 2 having a boiling point of from about −29° C. to about −28° C. at a pressure of about 14.5 psia.
 9. The azeotrope-like composition of claim 3 having a boiling point of from about −19.2° C. to about −18.9° C. at a pressure of about 14.5 psia.
 10. The azeotrope-like composition of claim 3 having a boiling point of from about −19.2° C. to about −19° C. at a pressure of about 14.5 psia.
 11. A sprayable composition comprising a material to be sprayed and a propellant comprising the azeotrope-like composition of claim
 1. 12. A refrigerant composition comprising the azeotrope-like composition of claim
 1. 13. A refrigeration system comprising the refrigerant of claim
 12. 14. A blowing agent comprising the azeotrope-like composition of claim
 1. 15. A foamable composition comprising the azeotrope-like composition of claim 1 and at least one thermoset foam component.
 16. The foamable composition of claim 15, wherein said at least one thermoset component comprises a composition capable of forming a polyurethane foam.
 17. The foamable composition of claim 15 wherein said at least one thermoset component comprises a composition capable of forming a polyisocyanurate foam.
 18. The foamable composition of claim 15 wherein said at least one thermoset component comprises a composition capable of forming a phenolic foam.
 19. A foamable composition comprising a mixture of an organic polyisocyanate and the polyol premix composition comprising a combination of a blowing agent, a polyol, a surfactant, and an amine catalyst, wherein the blowing agent comprises the azeotrope-like composition of claim 1 and optionally a hydrocarbon, halogenated hydrocarbon, CO₂ generating material, or combinations thereof.
 20. A foamable composition comprising the azeotrope-like composition of claim 1 and at least one thermoplastic foam component.
 21. The foamable composition of claim 20, wherein said at least one thermoplastic foam component comprises a thermoplastic polymer.
 22. The foamable composition of claim 21 wherein said thermoplastic polymer comprises a polystyrene, polyethylene, polypropylene, polyethyleneterephthalate, and combinations of these. 